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European Journal of Chemistry 5 (4) (2014) 681‐694

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European Journal of Chemistry 5 (4) (2014) 681‐694 European Journal of Chemistry 5 (4) (2014) 681‐694 European Journal of Chemistry Journal homepage: www.eurjchem.com Synthesis, reactions and applications of pyranotriazolopyrimidines Ashraf Hassan Fekry Abd El‐Wahab a,b,*, Ibrahim Ali Radini a and Hany Mostafa Mohamed a,b a Chemistry Department, Faculty of Science, Jazan University, 2097, Jazan, Saudi Arabia b Chemistry Department, Faculty of Science, Al‐Azhar University, 11884, Nasr City, Cairo, Egypt *Corresponding author at: Chemistry Department, Faculty of Science, Jazan University, 2097, Jazan, Saudi Arabia. Tel.: +966.054.0963753. Fax: +966.017.3230028. E‐mail address: [email protected] (A.H.F.A. El‐Wahab). REVIEW INFORMATION ABSTRACT This review deals with synthesis, reactions and their applications of pyranotriazolo‐ pyrimidines. The main purpose of this review is present a survey of literatures on the reactivity of amino imino derivatives and carboxylic acid derivatives. Some of these reactions have been applied successfully to the synthesis of biological important compounds. DOI: 10.5155/eurjchem.5.4.681‐694.1087 Received: 30 April 2014 Received in revised form: 27 May 2014 Accepted: 27 May 2014 Online: 31 December 2014 KEYWORDS Naphthols Pyrimidine Biological activity Pyranopyrimidines α‐Cyanocinnamonitriles Carboxylic acid derivatives 1. Introduction chemical and biological view points, due to their diverse pharmacological activities, such as antitumor potency [19,20], Pyran derivatives have attracted a great deal of interest inhibition of KDR kinase [21], antifungal effect [22] and owing to their antimicrobial activity [1‐7], inhibition of influ‐ macrophage activation [23]. enza, virus sialidase [8], mutagenic activity [9], activity as antiviral [10], anti‐proliferaction agents [11], sex pheromones [12], antitumor [13] and anti‐inflammatory agents [14]. The condensation of a ring of 1,2,4‐triazole and another one of pyrimidine gives rise to the formation of bicyclic hetero‐ cycles known as 1,2,4‐triazolopyrimidines. Four different possibilities exist for the relative orientation of both rings, so four different isomeric families of compounds are defined: 1,2,4‐triazolo[1,5‐a]pyrimidine (I), 1,2,4‐triazolo[1,5‐c]pyrimi‐ dine (II), 1,2,4‐triazolo[4,3‐a]pyrimidine (III) and 1,2,4‐ triazolo[4,3‐c]pyrimidine (V) (Figure 1). Among these isomeric families of compounds, 1,2,4‐ triazolo[1,5‐a]‐pyrimidine derivatives are thermodynamically more stable and, thus, the most studied ones [15], a few of them being commercially available. Revisions surveying the synthesis, reactivity, spectroscopic characterization and crystallographic studies of 1,2,4‐triazolo[1,5‐c]‐pyrimidines [16], 1,2,4‐triazolo[4,3‐a]pyrimidines [17] and 1,2,4‐triazolo Figure 1. Structures of triazolopyrimidines. [4,3‐c]pyrimidines [18] have also been published. From the standpoint of biological activity, fused hetero‐ They have proved to be promising anticancer agents with aromatic systems are often of much greater interest than the dual mechanisms of tubulin polymerization promotion [19,20] constituent monocyclic compounds. Recently, 1,2,4-triazolo as well as anti‐mycobacterial agents [24]. Some examples of [1,5‐a]pyrimidines have aroused increasing attention from the European Journal of Chemistry ISSN 2153‐2249 (Print) / ISSN 2153‐2257 (Online) 2014 Eurjchem Publishing ‐ Printed in the USA http://dx.doi.org/10.5155/eurjchem.5.4.681‐694.1087 682 El‐Wahab et al. / European Journal of Chemistry 5 (4) (2014) 681‐694 published derivatives of 1,2,4-triazolo[1,5‐a]pyrimidine with to proceed via bis(ethoxylcarbonyl) derivative [A] as their biological activities are as following. intermediate, which cyclized into compound 7 with elimination of ethanol (Scheme 2). 2. Synthesis of pyrano triazolo pyrimidine derivatives 2.1. Synthesis from 6‐methoxy‐2‐naphthol [25‐27] Condensation of 6‐methoxy‐2‐naphthol (1) with α‐ cyanocinnamonitriles (2a‐f) afforded the corresponding 2‐ amino‐4‐(aryl)‐7‐methoxy‐4H‐naphtho[2, 1‐b]pyran‐3‐carbo nitriles, 3a‐c, ethoxymethylene derivatives (4a‐c) was obtained by refluxing compounds 2‐amino‐4‐(aryl)‐7‐methoxy‐4H‐ naphtho[2,1‐b]pyran‐3‐carbonitriles (3a‐c) with triethyl ortho‐ formate as electrophile in the presence of acetic anhydride. Hydrazinolysis of ethoxymethylene derivatives 4a‐c in ethanol, at room temperature furnished the novel 10‐amino‐10,11‐ dihydro‐11‐imino‐3‐methoxy‐12‐(aryl)‐12H‐naphtho [2, 1‐b] pyrano[2,3‐d]pyrimidine derivatives 5a‐c in good yield. Reaction of aminoimino derivatives 5a‐c with formic acid or triethyl ortho‐formate affords the corresponding pyrano Scheme 2 triazolo‐pyrimidine derivative 6a. Also compounds 5a‐c reacted with acetylchloride and or benzoyl chloride gave the While treatment of 10‐amino‐10,11‐dihydro‐11‐imino‐3‐ corresponding 11‐methoxy‐2‐methyl/phenyl‐14‐(aryl)‐14H‐ methoxy‐12‐(p‐chloro/bromophenyl)‐12H‐naphtho [2, 1‐b] naphtho[2,1‐b]‐pyrano[2,3‐e][1,2,4]triazolo[1,5‐c]pyrimidines pyrano‐[2,3‐d] pyrimidine (5b,c) with ethylchloroformate in (6b,c), while cyclo‐condensation of compound 5a‐c with ethyl dry benzene afforded 11‐methoxy‐14‐(p‐chloro/bromo cyanoacetate or diethyl oxalate afforded the corresponding 2‐ phenyl)‐2‐oxo‐2H,3H,14H‐naphtho[2,1‐b]‐pyrano[3,2‐e][1,2,4] cyanomethyl and 2‐ethoxycarbonyl derivatives 6d and 6e, triazolo[1,5‐c]pyrimidines (8a,b). Reaction of compound 5b,c respectively (Scheme 1). with CS2/alc. KOH gave triazolo‐2‐thiones (8c,d), respectively, (Scheme 3). Scheme 3 2.2. Synthesis from 6‐bromo‐2‐naphthol [28,29] Condensation of various substituted α‐cyanocinnamo nitriles 2a,c with 6‐bromo‐2‐naphthol (10) in ethanolic piperidine afforded the corresponding 2‐amino‐4‐(aryl)‐7‐ bromo‐4H‐naphtho[2,1‐b]pyran‐3‐carbonitriles (11a‐e). Treat‐ ment of compounds 11a‐d with triethyl ortho‐formate in acetic anhydride at reflux gave the corresponding ethoxylmethylen amino derivatives 12a‐d. Hydrazinolysis of compounds 12a‐d in ethanol at room temperature afforded the imino derivatives 13a‐d. Interaction of compounds 13a,b with triethyl ortho‐ formate afforded 11‐bromo‐14‐(p‐tolyl or p‐methoxyphenyl)‐ 14H‐naphtho[1`,2`:5,6]pyrano[3,2‐e][1,2,4]triazolo[2,3‐c]pyri‐ midines (14a,b), respectively, (Scheme 4). Reaction of compounds 13a,b with acetyl chloride and ethyl cyano acetate at reflux the corresponding 2‐methyl‐14‐(p‐ tolyl or p‐methoxyphenyl)‐14H‐naphtho‐[2,1‐b]pyrano[2,3‐ e][1,2,4]triazolo[1,5‐c]pyrimidines (14c,d) and 2‐acetonitrile‐ 14‐ (p‐tolyl or p‐methoxyphenyl)‐14H‐naphtho[2,1‐b] pyrano‐ [2,3‐e][1,2,4]triazolo[1,5‐c]pyrimidines (14e,f), respectively, were formed. Reaction of compounds 13a,b with diethyl oxalate and benzoyl chloride at reflux afforded the correspond‐ ding 2‐ethoxycarbonyl 14g,h and 2‐phenyl 14i,j derivatives. Scheme 1 Reaction of compound 13a with methyl or ethyl chloroformate (1 mole) in dry benzene afforded the 1:1 adduct triazol‐2‐one Treatment of 10‐amino‐10,11‐dihydro‐11‐imino‐3‐met‐ 15, Instead of the anticipated formation of the triazolo hoxy‐12‐(p‐tolyl)‐12H‐naphtho[2,1‐b]pyrano[2,3‐d]pyrimidine pyrimidine derivative 15 the reaction of compound 13d with (5a) with two moles of ethylchloroformate in dry benzene methyl or ethyl chloroformate in dry benzene afforded 16, afforded 1:2 adduct 7. Formation of compound 7 was assumed through nucleophilic displacement followed by spontaneous El‐Wahab et al. / European Journal of Chemistry 5 (4) (2014) 681‐694 683 Scheme 4 hydrolysis of the ester intermediate [B] into the corresponding chloride, benzoyl chloride, ethyl cyanoacetate, diethyl oxalate carbamic acid derivative 16. Interaction of compound 13a,d afforded the corresponding triazolopyrimidine derivatives with benzaldehydes in dioxane/piperidine afforded 14j and 21a‐e (Scheme 6). dihydrotriazolopyrimidine derivative 17 and non‐isolable 14i, respectively, (Scheme 5). Scheme 5 Scheme 6 2.3. Synthesis from 2‐naphthol [30] 2.4. Synthesis from naphtho[2,1‐b]pyrans [31] Condensation of α‐cyanocinnamonitrile 2a, with 2‐ Reaction of 2‐amino 4‐aryl‐3‐cyano‐4H‐naphtho[2,1‐ naphthol in ethanolic piperidine afforded 2‐amino‐4‐(p‐tolyl)‐ b]pyrans 18 and 22 with triethyl ortho‐formate, triethyl ortho‐ 4H‐naphtho[2,1‐b]‐pyran‐3‐carbonitrile (18). Treatment of acetate or triethyl ortho‐propionate in 1,4‐dioxane, in presence compound 18 with triethyl ortho‐formate in acetic anhydride amount of acetic acid under reflux to give 2‐[(ethoxy at reflux gave the corresponding ethoxylmethylenamino alkylidene)amino‐4‐aryl‐3‐cyano‐4H‐naphtho‐[2,1‐b]pyrans 19 derivative 19. Hydrazinolysis of compound 19 in ethanol at and 23, respectively, (Scheme 7). room temperature afforded the imino derivative 20. Interaction of compound 20 with triethyl ortho‐formate, acetyl 684 El‐Wahab et al. / European Journal of Chemistry 5 (4) (2014) 681‐694 cyclisation via elimination of water to give pyrano triazolo‐ pyrimidine, 27. H OEt Ar NH Ar N N-Ts NHTs HC(OEt)3 N N O N R O N R 24a) Ar = C6H5 R=H [C] b) Ar = p-CH3-C6H4 R=H d) Ar = p-Cl-C6H4 R=H -EtOTs f) Ar = p-CH3-C6H4 R=CH3 g) Ar = o-CH3O-C6H4 R=CH3 l) Ar = o-CH3O-C6H4 R=Et 12 m) Ar = p-Cl-C6H4 R=Et 1 2 13 11 Ar N 10 N 3 14 N 4 O Scheme 7 9 O N 5 R S 8 O 7 6 O The reaction of these imidates 19 and 23, with tosyl Ethyl 4-methyl benzenesulfonate 21a) Ar = p-CH3-C6H4 R=H hydrazine, in toluene at reflux and few drops of acetic acid, 25a) Ar = C6H5 R=H afforded the desired key intermediate N1‐tosylamino‐11‐aryl‐ d) Ar = p-Cl-C6H4 R=H 1,12‐dihydro‐11H‐naphthopyrano‐[2, 3‐d]pyrimidine (24) f) Ar = p-CH3-C6H4 R=CH3 g) Ar = o-CH3O-C6H4 R=CH3 (Scheme 8).
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